HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dimethoxy-5-nitrobenzhydrol → 3,4-Dimethoxy-5-nitrobenzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dimethoxy-5-nitrobenzhydrol | HCID 21458992 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,4-Dimethoxy-5-nitrobenzophenone | HCID 21459055 | — |
Reaction Steps
2.5 g of 3,4-dimethoxy-5-nitrobenzhydrol dissolved in 50 ml of methylene chloride are treated with 2.2 g of pyridinium chlorochromate, whereupon the mixture is stirred at room temperature for 2 hours. The insoluble constituents are subsequently filtered. The filtrate is evaporated and the residue is chromatographed on 60 g of silica gel with methylene chloride. After crystallization from methylene chloride/hexane there is obtained 3,4-dimethoxy-5-nitrobenzophenone of m.p. 78°-80°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705703 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-a29d2c126e144140873b71ef1548f5bc |
| Source note | uspto-grants-1998_01 |